Cargando…
HFE Gene Polymorphisms and the Risk for Autism in Egyptian Children and Impact on the Effect of Oxidative Stress
Background: Autism is among the commonest neurodevelopmental childhood disorders worldwide; its aetiology is still unknown. Iron metabolism alteration in the central nervous system is recently implicated as a risk factor for several neurodegenerative disorders. Haemochromatosis HFE gene polymorphism...
Autores principales: | Gebril, Ola H., Meguid, Nagwa A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826890/ https://www.ncbi.nlm.nih.gov/pubmed/22048270 http://dx.doi.org/10.3233/DMA-2011-0830 |
Ejemplares similares
-
A study of blood serotonin and serotonin transporter promoter variant (5-HTTLPR) polymorphism in Egyptian autistic children
por: Meguid, Nagwa A., et al.
Publicado: (2015) -
MTHFR Genetic Polymorphism As a Risk Factor in Egyptian Mothers with Down Syndrome Children
por: Meguid, Nagwa A., et al.
Publicado: (2008) -
Screening of Dystrophin Gene Deletions in Egyptian Patients with DMD/BMD Muscular Dystrophies
por: Effat, Laila K., et al.
Publicado: (2000) -
Polymorphism in Variable Number of Tandem Repeats of Dopamine D4 Gene Is a Genetic Risk Factor in Attention Deficit Hyperactive Egyptian Children: Pilot Study
por: Shahin, Ola, et al.
Publicado: (2015) -
Expression of Reactive Oxygen Species–Related Transcripts in Egyptian Children With Autism
por: Meguid, Nagwa A, et al.
Publicado: (2017)